- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07715812
E-diary vs Paper Diary in Binge Eating Disorder (A-3650-0001)
A Mixed Methods, Observational, Cross-over Study of Measurement Comparability and Usability of Electronic and Paper Formats of a Binge Eating Diary
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Binge eating (BE) diary has already been successfully employed to measure binge eating behavior in clinical trials. This has been implemented using a paper diary (p-diary) completed daily in the evening. From the diary records, binge eating episodes are confirmed by a healthcare professional. Despite the advantages of electronic implementation and the clinical and research need for such a tool, no electronic diary (e-diary) has been systematically tested in comparison to paper diary through an empirical study.
The following scientific questions are to be answered with this project
- Are the paper and electronic diary formats considered measurement comparable, such that data collected using the different formats across different studies or programs could be directly comparable?
- Are there differences in usability that might limit completion rates or lead to under reporting using one or the other mode of data collection?
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Anna I Guerdjikova, PhD,LISW, PhD,LISW
- Telefonnummer: 5135360700
- E-post: anna.guerdjikova@lindnercenter.org
Studiesteder
-
-
Ohio
-
Mason, Ohio, Forente stater, 45040
- Rekruttering
- Lindner Center of Hope
-
Ta kontakt med:
- Aspen Madrid, MS
- Telefonnummer: 5135360714
- E-post: aspen.madrid@lindnercenter.org
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Diagnosis of Binge Eating Disorder based on The Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) (5) criteria (as assessed with BED module of the structural clinical interview [SCID] (6) for DSM-5)
- Reported frequency of minimum of 2 binge episodes/week
- Age: over 18 years of age
- Ability to understand and complete self-reporting measures 5 . The subject owns a smartphone compatible with Google Play or Apple App Store and is able to download and use apps appropriately.
Exclusion Criteria:
- Comorbid psychiatric conditions requiring immediate hospitalization (as assessed with MSE)
- IInability to use smartphone or paper diary due to physical limitations or technical barriers (e.g., severe visual impairment)
- Inability to read/write in English
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Annen: paper diary arm
subjects will complete paper diary for 2 weeks
|
complete paper diary for 2 weeks
|
|
Annen: e-diary arm
subjects will complete e-diary for 2 weeks
|
The subject will complete one diary format and switch to the other after 2 weeks
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
The primary endpoint is the comparison of number of binge eating episodes recorded over a 14-day period between diary formats
Tidsramme: from enrollment v1,day 0 to v3,day 30
|
The primary endpoint is the comparison of number of binge eating episodes recorded over a 14-day period between diary formats
|
from enrollment v1,day 0 to v3,day 30
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- A-3650-0001
Plan for individuelle deltakerdata (IPD)
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